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帕博西尼联合芳香化酶抑制剂作为晚期/转移性乳腺癌一线治疗的真实世界治疗模式和临床疗效:来自美国 Syapse 学习健康网络的分析。

Real-World Treatment Patterns and Clinical Effectiveness of Palbociclib Plus an Aromatase Inhibitor as First-Line Therapy in Advanced/Metastatic Breast Cancer: Analysis from the US Syapse Learning Health Network.

机构信息

Syapse, San Francisco, CA 94107, USA.

Pfizer Inc., New York, NY 10017, USA.

出版信息

Curr Oncol. 2022 Feb 12;29(2):1047-1061. doi: 10.3390/curroncol29020089.

Abstract

This retrospective single-arm study assessed real-world treatment patterns and clinical outcomes in patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced/metastatic breast cancer (A/MBC) who received palbociclib plus an aromatase inhibitor as first-line therapy in US community health systems. Using electronic health records from the Syapse Learning Health Network, 242 patients were identified as having received first-line palbociclib plus an aromatase inhibitor between 3 February 2015, and 31 July 2019 (data cutoff 1 February 2020) resulting in a minimum potential 6-month follow-up period. In total, 56.6% of patients had de novo A/MBC at initial breast cancer diagnosis, 50.8% had bone-only disease, and 32.2% had visceral disease. Median follow-up was 22.4 months. Disease progression (26.4%) and intolerance/toxicity (14.9%) were the main reasons for treatment discontinuation. The median (95% CI) real-world progression-free survival was 31.7 (27.9-not estimable (NE)) months and 2-year estimated overall survival (OS) rate was 78.0%. In total, 25.6% of patients died; however, OS data are limited by the small population size and insufficient follow-up time. These real-world effectiveness outcomes complement findings from other real-world studies and randomized controlled trials and support palbociclib plus an aromatase inhibitor as first-line therapy for HR+/HER2- A/MBC.

摘要

这项回顾性单臂研究评估了在美国社区卫生系统中接受哌柏西利联合芳香化酶抑制剂作为一线治疗的激素受体阳性/人表皮生长因子受体 2 阴性(HR+/HER2-)晚期/转移性乳腺癌(A/MBC)患者的真实世界治疗模式和临床结局。使用来自 Syapse 学习健康网络的电子健康记录,在 2015 年 2 月 3 日至 2019 年 7 月 31 日(数据截止日期为 2020 年 2 月 1 日)期间,共确定了 242 例接受一线哌柏西利联合芳香化酶抑制剂治疗的患者,这导致了最小的潜在 6 个月随访期。总的来说,56.6%的患者在初始乳腺癌诊断时患有新发 A/MBC,50.8%的患者有骨转移,32.2%的患者有内脏转移。中位随访时间为 22.4 个月。疾病进展(26.4%)和不耐受/毒性(14.9%)是停止治疗的主要原因。中位(95%CI)真实世界无进展生存期为 31.7(27.9-无法估计(NE))个月,2 年估计总生存率(OS)为 78.0%。共有 25.6%的患者死亡;然而,由于人口规模小和随访时间不足,OS 数据有限。这些真实世界的疗效结果补充了其他真实世界研究和随机对照试验的结果,并支持哌柏西利联合芳香化酶抑制剂作为 HR+/HER2-A/MBC 的一线治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4414/8871271/d1d8723d80d3/curroncol-29-00089-g001.jpg

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